Parkinson Disease and Melanoma: A Common Genetic Pathway Linked to PARKIN Inactivation

被引：0

作者：

Hu, H-H ^{[1
]}

Lesage, S. ^{[2
]}

Michel, L. ^{[3
]}

Descamps, V ^{[3
]}

Mourah, S. ^{[3
]}

Lebbe, C. ^{[3
]}

Basset-Seguin, N. ^{[3
]}

Bagot, M. ^{[3
]}

Bensussan, A. ^{[3
]}

Deschamps, L. ^{[4
]}

Leccia, M. T. ^{[5
]}

Sivaramakrishna, R. P. ^{[6
]}

Klebe, S. ^{[2
]}

Kumar, R. ^{[6
]}

Kannengiesser, C. ^{[7
]}

Couvelard, A. ^{[4
]}

Thomas, L. ^{[8
]}

Brice, A. ^{[2
]}

Dumaz, N. ^{[3
]}

Grandchamp, B. ^{[7
]}

Nadem, S. ^{[1
]}

机构：

[1] Univ Paris 07, Bichat Hosp, APHP, INSERM,Genet Dept,U976, Paris, France

[2] Univ Paris 06, INSERM, Hop La Pitie Salpetriere, AP HP,UMR S975,Ctr Rech,Inst Cerveau & Moelle Epi, Paris, France

[3] Univ Paris 07, INSERM, U976, Skin Res Ctr, Paris, France

[4] Univ Paris 07, Dept Pathol, Bichat Hosp, APHP, Paris, France

[5] CHU Grenoble, Dept Dermatol, F-38043 Grenoble, France

[6] German Canc Res Ctr, Div Mol Genet Epidemiol, Heidelberg, Germany

[7] Univ Paris 07, Dept Genet, Bichat Hosp, APHP, Paris, France

[8] Univ Lyon 1, Dept Dermatol, Ctr Hosp Lyon Sud, F-69365 Lyon, France

来源：

JOURNAL DER DEUTSCHEN DERMATOLOGISCHEN GESELLSCHAFT | 2013年 / 11卷

关键词：

D O I：

暂无

中图分类号：

R75 [皮肤病学与性病学];

学科分类号：

100206 ;

摘要：

引用

页码：47 / 47

页数：1

共 50 条

[21] Parkinson's disease - do patients with parkin gene mutations share a common phenotype?
Moreira, F.
Almeida, R.
Januario, C.
JOURNAL OF NEUROLOGY, 2010, 257 : S215 - S216
[22] Citation Classic Parkin and Parkinson Disease
Shimura, Hideki
Mizuno, Yoshikuni
Hattori, Nobutaka
CLINICAL CHEMISTRY, 2012, 58 (08) : 1260 - 1261
[23] Parkin function in Parkinson's disease
Arkinson, Connor
Walden, Helen
SCIENCE, 2018, 360 (6386) : 267 - 268
[24] Genetics of parkin-linked disease
West, AB
Maidment, NT
HUMAN GENETICS, 2004, 114 (04) : 327 - 336
[25] Genetics of parkin-linked disease
Andrew B. West
Nigel T. Maidment
Human Genetics, 2004, 114 : 327 - 336
[26] The role of common genetic risk variants in Parkinson disease
Tan, E-K
CLINICAL GENETICS, 2007, 72 (05) : 387 - 393
[27] Nigral degeneration and striatal dopaminergic dysfunction in idiopathic and Parkin-linked Parkinson's disease
Hu, MTM
Scherfle, C
Khan, NL
Hajnal, JV
Lees, AJ
Quinn, N
Wood, NW
Brooks, DJ
MOVEMENT DISORDERS, 2006, 21 (03) : 299 - 305
[28] Parkinson’s disease-linked Parkin mutations impair glutamatergic signaling in hippocampal neurons
Mei Zhu
Giuseppe P. Cortese
Clarissa L. Waites
BMC Biology, 16
[29] PTEN-induced kinase 1 (PINK1) and Parkin: Unlocking a mitochondrial quality control pathway linked to Parkinson's disease
Agarwal, Shalini
Muqit, Miratul M. K.
CURRENT OPINION IN NEUROBIOLOGY, 2022, 72 : 111 - 119
[30] The Parkinson's disease–linked proteins Fbxo7 and Parkin interact to mediate mitophagy
Victoria S Burchell
David E Nelson
Alvaro Sanchez-Martinez
Marta Delgado-Camprubi
Rachael M Ivatt
Joe H Pogson
Suzanne J Randle
Selina Wray
Patrick A Lewis
Henry Houlden
Andrey Y Abramov
John Hardy
Nicholas W Wood
Alexander J Whitworth
Heike Laman
Helene Plun-Favreau
Nature Neuroscience, 2013, 16 : 1257 - 1265

← 1 2 3 4 5 →